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游离脂肪酸作为大鼠脂肪细胞中腺苷酸环化酶和环3',5'-AMP积累的反馈调节因子。

Free fatty acids as feedback regulators of adenylate cyclase and cyclic 3':5'-AMP accumulation in rat fat cells.

作者信息

Fain J N, Shepherd R E

出版信息

J Biol Chem. 1975 Aug 25;250(16):6586-92.

PMID:169252
Abstract

Rat fat cells incubated with lipolytic agents released substances to the medium which acted as feedback regulators of cyclic adenosine 3':5'-monophosphate (cyclic AMP) accumulation. The feedback regulators were not removed by adenosine deaminase. Dialyzed medium that had previously been incubated with fat cells in the presence of norepinephrine markedly inhibited cyclic AMP accumulation by fresh cells, whereas dialyzed medium from control cells did not inhibit cyclic AMP accumulation. The effects of lipolytic agents could be mimicked by adding dialyzed medium previously incubated with fat cells in the presence of oleic acid. This suggested that free fatty acids were the nondialyzable and adenosine deaminase-insensitive inhibitors of cyclic AMP accumulation released to the medium by fat cells incubated with lipolytic agents. The regulatory function of free fatty acids was related to the molar ratio of fatty acid to albumin. Profound inhibition of both lipolysis and cyclic AMP accumulation was seen as the free fatty acid/albumin ratio exceeded 3. The inhibition of cyclic AMP accumulation by oleate was seen as soon as there was a detectable increase in cyclic AMP due to lipolytic agents. Protein kinase activity (in the presence of cyclic AMP) of the infranatant obtained after centrifugation of fat cell homogenates at 48,000 x g was inhibited by medium from cells incubated with lipolytic agents or added oleate. Adenylate cyclase activity of rat fat cell ghosts was also inhibited by dialyzed or nondialyzed medium that previously had been incubated with lipolytic agents or added fatty acids. The direct addition of oleate markedly inhibited adenylate cyclase activity as the free fatty acid/albumin ratio exceeded 2. These data suggest that the prolonged drop in cyclic AMP accumulation seen during the incubation of rat fat cells with lipolytic agents is due to the inhibition of adenylate cyclase. This occurs when the free fatty acid/albumin ratio exceeds 3.

摘要

用脂解剂孵育的大鼠脂肪细胞向培养基中释放了一些物质,这些物质作为环磷酸腺苷(cAMP)积累的反馈调节因子发挥作用。腺苷脱氨酶不能去除这些反馈调节因子。先前在去甲肾上腺素存在下与脂肪细胞一起孵育的透析培养基显著抑制新鲜细胞的cAMP积累,而来自对照细胞的透析培养基则不抑制cAMP积累。通过添加先前在油酸存在下与脂肪细胞一起孵育的透析培养基,可以模拟脂解剂的作用。这表明游离脂肪酸是用脂解剂孵育的脂肪细胞释放到培养基中的不可透析且对腺苷脱氨酶不敏感的cAMP积累抑制剂。游离脂肪酸的调节功能与脂肪酸与白蛋白的摩尔比有关。当游离脂肪酸/白蛋白比值超过3时,脂解和cAMP积累均受到显著抑制。一旦由于脂解剂导致cAMP有可检测到的增加,就会观察到油酸对cAMP积累的抑制作用。在48,000×g离心脂肪细胞匀浆后获得的上清液中的蛋白激酶活性(在cAMP存在下)受到用脂解剂孵育的细胞培养基或添加油酸的抑制。大鼠脂肪细胞膜微粒体的腺苷酸环化酶活性也受到先前与脂解剂孵育或添加脂肪酸的透析或未透析培养基的抑制。当游离脂肪酸/白蛋白比值超过2时,直接添加油酸会显著抑制腺苷酸环化酶活性。这些数据表明,在用脂解剂孵育大鼠脂肪细胞期间观察到的cAMP积累的长期下降是由于腺苷酸环化酶受到抑制。当游离脂肪酸/白蛋白比值超过3时就会发生这种情况。

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